The Immune Status of Patients with 16p11.2 Deletion Syndrome

被引:1
|
作者
Wang, Laura A. [1 ,2 ]
Larson, Austin [1 ,2 ]
Abbott, Jordan K. [1 ,2 ]
机构
[1] Childrens Hosp Colorado, 13123 16th Ave, Aurora, CO 80045 USA
[2] Univ Colorado, 13123 16th Ave, Aurora, CO 80045 USA
关键词
D O I
10.1007/s10875-023-01597-2
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
引用
收藏
页码:1792 / 1795
页数:4
相关论文
共 50 条
  • [1] The Immune Status of Patients with 16p11.2 Deletion Syndrome
    Laura A. Wang
    Austin Larson
    Jordan K. Abbott
    Journal of Clinical Immunology, 2023, 43 : 1792 - 1795
  • [2] 16p11.2 deletion syndrome
    Chung, Wendy K.
    Roberts, Timothy P. L.
    Sherr, Elliott H.
    Snyder, LeeAnne Green
    Spiro, John E.
    CURRENT OPINION IN GENETICS & DEVELOPMENT, 2021, 68 : 49 - 56
  • [3] Sensory processing in 16p11.2 deletion and 16p11.2 duplication
    Smith, Harriet
    Lane, Chloe
    Al-Jawahiri, Reem
    Freeth, Megan
    AUTISM RESEARCH, 2022, 15 (11) : 2081 - 2098
  • [4] Cognitive and Behavioral Characterization of 16p11.2 Deletion Syndrome
    Hanson, Ellen
    Nasir, Ramzi H.
    Fong, Alexa
    Lian, Alyss
    Hundley, Rachel
    Shen, Yiping
    Wu, Bai-Lin
    Holm, Ingrid A.
    Miller, David T.
    JOURNAL OF DEVELOPMENTAL AND BEHAVIORAL PEDIATRICS, 2010, 31 (08): : 649 - 657
  • [5] A case with a 552 kb deletion syndrome at 16p11.2
    Duymus, Fahrettin
    Esin, Deniz
    Tulgar, Busra Goksel
    Kocak, Nadir
    Cora, Tulun
    MOLECULAR GENETICS AND METABOLISM, 2021, 132 : S159 - S160
  • [6] A Hypothesis: Metabolic Contributions to 16p11.2 Deletion Syndrome
    Choo, Brandon Kar Meng
    Barnes, Sarah
    Sive, Hazel
    BIOESSAYS, 2025, 47 (03)
  • [7] Phenotype variability in thirteen 16p11.2 deletion patients
    Roda, Diana
    Gabau, Elisabeth
    Baena, Neus
    Guitart, Miriam
    ANALES DE PEDIATRIA, 2018, 89 (01): : 62 - 63
  • [8] Hyperinsulinaemic hypoglycaemia: A new presentation of 16p11.2 deletion syndrome
    Kostopoulou, Eirini
    Dastamani, Antonia
    Caiulo, Silvana
    Antell, Hannah
    Flanagan, Sarah E.
    Shah, Pratik
    CLINICAL ENDOCRINOLOGY, 2019, 90 (05) : 766 - 769
  • [9] 16p11.2 Deletion Syndrome in Prenatal Diagnosis - a rare case
    Freitas, Manuela Mota
    Candeias, Cristina
    Pires, Silvia
    Oliva-Teles, Natalia
    Tavares, Purificacao
    Rodrigues, Maria Do Ceu
    Fonseca E Silva, Maria Da Luz
    MOLECULAR CYTOGENETICS, 2017, 10
  • [10] Language and Communication Deficits in Chromosome 16p11.2 Deletion Syndrome
    Salud Jimenez-Romero, Ma
    Fernandez-Urquiza, Maite
    Benitez-Burraco, Antonio
    JOURNAL OF SPEECH LANGUAGE AND HEARING RESEARCH, 2022, 65 (12): : 4724 - 4740